Water → 4,5-Bis(4-methoxybutyryloxy)-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid
Reaktionsgleichung
[OH:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][C:12]=3[OH:17])[C:7](=[O:18])[C:6]=2[CH:5]=[C:4]([C:19]([OH:21])=[O:20])[CH:3]=1.[CH3:22][O:23][CH2:24][CH2:25][CH2:26][C:27](Cl)=[O:28].[OH2:30].[C:31]([O:34][CH2:35][CH3:36])(=O)C.N1[CH:42]=[CH:41]C=CC=1>>[CH3:22][O:23][CH2:24][CH2:25][CH2:26][C:27]([O:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][C:12]=3[O:17][C:41](=[O:30])[CH2:42][CH2:36][CH2:35][O:34][CH3:31])[C:7](=[O:18])[C:6]=2[CH:5]=[C:4]([C:19]([OH:21])=[O:20])[CH:3]=1)=[O:28]Komponenten
6
Versuchsvorschrift
To a stirred suspension of 4,5-dihydroxy-9,10-dioxoanthracene-2-carboxylic acid (1 g) in pyridine (30 ml) was added 4-methoxybutyryl chloride (2 g). The reaction was stirred at RT for 2 days, and as TLC indicated that starting acid was still present, a further 2 g of the acid chloride was added. Reaction was complete after a further 2 days at RT. The reaction mixture was evaporated to dryness and stirred in 2M HCl (30 ml) for 30 mins. The resultant crude solid was isolated by filtration. This was then slurried with water (30 ml) followed by ethyl acetate (30 ml). The solid was isolated by filtration and oven dried overnight to give 1.0 g (59%).
Aufarbeitung
- customReaction
- waitwas complete after a further 2 days at RT
- customThe reaction mixture was evaporated to dryness
- stirringstirred in 2M HCl (30 ml) for 30 mins
- customThe resultant crude solid was isolated by filtration
- customThe solid was isolated by filtration and oven
- customdried overnight
- customto give 1.0 g (59%)
Quellen und Nachweise
- ORD-Eintrag
- ord-73c404b0ec0942aba635c345255846ec
- Quelldatensatz
- uspto-grants-2010_06
- Patentnummer
- US07728035B2
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